Beilstein J. Org. Chem.
 2015
DOI: 10.3762/bjoc.11.214
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Aerobic addition of secondary phosphine oxides to vinyl sulfides: a shortcut to 1-hydroxy-2-(organosulfanyl)ethyl(diorganyl)phosphine oxides

С. Ф. Малышева1,
Alexander V. Artem’ev2,
Н. К. Гусарова3
et al.

Abstract: SummarySecondary phosphine oxides react with vinyl sulfides (both alkyl- and aryl-substituted sulfides) under aerobic and solvent-free conditions (80 °C, air, 7–30 h) to afford 1-hydroxy-2-(organosulfanyl)ethyl(diorganyl)phosphine oxides in 70–93% yields.

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Cited by 9 publications
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ChemInform Abstract: Aerobic Addition of Secondary Phosphine Oxides to Vinyl Sulfides: A Shortcut to 1‐Hydroxy‐2‐(organosulfanyl)ethyl(diorganyl)phosphine Oxides.

Малышева
1
,
Artem’ev
2
,
Гусарова
3
et al. 2015
ChemInform
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0
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ChemInform Abstract: Aerobic Addition of Secondary Phosphine Oxides to Vinyl Sulfides: A Shortcut to 1‐Hydroxy‐2‐(organosulfanyl)ethyl(diorganyl)phosphine Oxides.

Малышева
1
,
Artem’ev
2
,
Гусарова
3
et al. 2015
ChemInform
0
0
0
0
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Decarbonylation of Salicylaldehyde Activated byp‐Cymene Ruthenium(II) Dimer: Implication for Catalytic Alkyne Hydrothiolation

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,
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,
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et al. 2016
Eur J Org Chem
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Catalyst‐ and Solvent‐Free Hydrophosphorylation of Aldimines with Secondary Phosphine Chalcogenides: Synthesis of Tertiary α‐Aminophosphine Oxides, Sulfides and Selenides

Arbuzova
1
,
Verkhoturova
2
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Зинченко
3
et al. 2022
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